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rs180177164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs180177164(-;-)
Make rs180177164(-;CG)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878767
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177164
ebirs180177164
HLIrs180177164
Exacrs180177164
Varsomers180177164
Maprs180177164
PheGenIrs180177164
hapmaprs180177164
1000 genomesrs180177164
hgdprs180177164
ensemblrs180177164
gopubmedrs180177164
geneviewrs180177164
scholarrs180177164
googlers180177164
pharmgkbrs180177164
gwascentralrs180177164
openSNPrs180177164
23andMers180177164
23andMe allrs180177164
SNP Nexus

SNPshotrs180177164
SNPdbers180177164
MSV3drs180177164
GWAS Ctlgrs180177164
Max Magnitude0
ClinVar
Risk rs180177164(;)
Alt rs180177164(;)
Reference rs180177164(CG;CG)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241818184_241818185delCG
CLNSRC
CLNACC RCV000186419.1,